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Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomas.

AbstractPURPOSE:
Anaplastic gliomas constitute a heterogeneous group of tumors with different therapeutic responses to adjuvant chemotherapy with alkylating agents. O6-Methylguanine-DNA methyltransferase (MGMT), a DNA repair protein, is one of the implicated factors in glioma chemoresistance. The prognostic value of MGMT remains controversial due in part to the fact that previous published studies included heterogeneous groups of patients with different tumor grades. The aim of this study was to evaluate the prognostic significance of MGMT in patients with anaplastic glioma.
EXPERIMENTAL DESIGN:
Ninety-three patients with anaplastic glioma were analyzed for MGMT protein expression by immunohistochemistry. In addition, for those patients from whom a good yield of DNA was obtained (n = 40), MGMT promoter methylation profile was analyzed by methylation-specific PCR. MGMT prognostic significance was evaluated together with other well-known prognostic factors.
RESULTS:
Fifty-one tumors (54.8%) showed nuclear staining of MGMT. There was a trend towards longer overall survival for those patients with negative MGMT immunostaining (hazard ratio, 1.66; P = 0.066). In a secondary analysis including those patients who actually received chemotherapy (n = 72), the absence of MGMT expression was independently associated with better survival (hazard ratio, 2.12; P = 0.027). MGMT promoter methylation was observed in 50% of the analyzed tumors. No statistical correlation between MGMT expression and MGMT promoter hypermethylation was observed.
CONCLUSIONS:
Unlike previous studies, we did not find a correlation between MGMT promoter methylation and survival. However, we observed a correlation between MGMT protein expression and survival in those patients who received chemotherapy thus suggesting that the absence of MGMT expression is a positive predictive marker in patients with anaplastic glioma.
AuthorsMarta Brell, Avelina Tortosa, Eugenia Verger, Juan Miguel Gil, Nuria Viñolas, Salvador Villá, Juan José Acebes, Lluis Caral, Teresa Pujol, Isidro Ferrer, Teresa Ribalta, Francesc Graus
JournalClinical cancer research : an official journal of the American Association for Cancer Research (Clin Cancer Res) Vol. 11 Issue 14 Pg. 5167-74 (Jul 15 2005) ISSN: 1078-0432 [Print] United States
PMID16033832 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • O(6)-Methylguanine-DNA Methyltransferase
Topics
  • Adolescent
  • Adult
  • Aged
  • Brain Neoplasms (genetics, pathology)
  • DNA Methylation
  • Female
  • Follow-Up Studies
  • Gene Expression Profiling
  • Glioma (genetics, pathology)
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • O(6)-Methylguanine-DNA Methyltransferase (biosynthesis, genetics)
  • Polymerase Chain Reaction
  • Prognosis
  • Promoter Regions, Genetic
  • Survival Analysis

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